I am trying to use the galaxy &quot;BED to GFF&quot; function.  The operation worked, but instead of giving me back any feature information (e.g., exon, intron, repeat, etc.); I just received back the sequence of the interval contained within the BED file.  Does anyone know what I&#39;m doing wrong?  Moreover, does anyone know the best way to map each read of a RNAseq run to a given feature?  <br>
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